Loading...
Please wait, while we are loading the content...
Direct arylation of sydnones with aryl chlorides toward highly substituted pyrazoles.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Brown, Andrew W. Harrity, Joseph P. A. |
| Copyright Year | 2015 |
| Abstract | The direct arylation of the C4 position of both N-alkyl- and N-arylsydnones with aryl/heteroaryl chlorides has been realized. The reaction is quite general and allows access to a wide range of 4-substituted sydnones. Yields of more challenging substrates can be improved through the use of aryl bromides. |
| File Format | PDF HTM / HTML |
| DOI | 10.1021/acs.joc.5b00143 |
| PubMed reference number | 25635522 |
| Journal | Medline |
| Volume Number | 80 |
| Issue Number | 4 |
| Alternate Webpage(s) | http://eprints.whiterose.ac.uk/88792/3/WRRO_88792.pdf |
| Alternate Webpage(s) | https://doi.org/10.1021/acs.joc.5b00143 |
| Journal | The Journal of organic chemistry |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |